FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CC-100 CLOCK/CALANDER MODULE ACCESS. FOR G-2000 EL

K Number: K851633 · Decision Jun 26, 1985
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
15
Review Days
69

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CC-100 CLOCK/CALANDER MODULE ACCESS. FOR G-2000 EL
K Number
K851633
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Eaton Medical Group
Date Received
April 18, 1985
Decision Date
June 26, 1985
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPS Electrocardiograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DPS), ordered by most recent decision date.

View all

Other Clearances by Eaton Medical Group

K Number Device Name
K851623 MODEL TRC-40 TELEMETRY RECIEVER MODULE
K851624 MODEL TT-185 TELEMETRY TRANSMITTER
K851625 SCX-10 SINGLE CHANNEL RECORDER ACCESS. FOR G-2000
K851627 KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR
K851632 PCX-100 PATIENT INPUT LEADWIRE
K851631 TMX-C1/C2 TRADMILL CONTROLLER ACCESS.
K851630 TMX-80 TREADMILL
K851629 TMX-70 TREADMILL
K851628 RMG-9 9 REMOTE MONITOR ACCESS. FOR G-2000 ELECTRO
K851626 SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE
Search all 15 clearances from Eaton Medical Group →